Cas 55682-56-9,Acetic acid (1R,2S,3R,4R,5R)-4-azido-3-hydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yl ester

55682-56-9

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Basic information

Product Name: Acetic acid (1R,2S,3R,4R,5R)-4-azido-3-hydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yl ester
Synonyms:
CAS NO:55682-56-9
Molecular Formula:
Molecular Weight: 229.192
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Acetic acid (1R,2S,3R,4R,5R)-4-azido-3-hydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (1R,2S,3R,4R,5R)-4-azido-3-hydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yl ester(55682-56-9)
EPA Substance Registry System: Acetic acid (1R,2S,3R,4R,5R)-4-azido-3-hydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yl ester(55682-56-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 55682-56-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 55682-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,8 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55682-56:
(7*5)+(6*5)+(5*6)+(4*8)+(3*2)+(2*5)+(1*6)=149
149 % 10 = 9
So 55682-56-9 is a valid CAS Registry Number.

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55682-56-9Downstream Products

55682-56-9Relevant academic research and scientific papers

Facile Preparation of 3,4-Di-O-acetyl-1,6-anhydro-2-azido-2-deoxy-β-D-glucopyranose and Some Derivatives Thereof: Useful Precursors for Oligosaccharide Synthesis

Dasgupta, Falguni,Garegg, Per J.

, p. 626 - 628 (1988)

A facile, virtually one-pot synthesis of the title compound and also some of its derivatives is based on regioselective 2-substitutions of 1,6-anhydro-β-D-mannopyranose using stannylidene activation.The compounds thus prepared are useful precursors in the synthesis of glycoprotein-type oligosaccharides.

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